vha-16

Caenorhabditis elegans

Predicted to enable proton-transporting ATPase activity, rotational mechanism. Predicted to be involved in vacuolar acidification and vacuolar transport. Predicted to be located in early endosome. Predicted to be part of plasma membrane proton-transporting V-type ATPase complex and vacuolar proton-transporting V-type ATPase complex. Expressed in head and tail. Is an ortholog of human ATP6V0D1 (ATPase H+ transporting V0 subunit d1).

F25B4.8

Caenorhabditis elegans

Predicted to enable carbon-sulfur lyase activity and metal ion binding activity. Is an ortholog of human CENPV (centromere protein V).

F02E9.1

Caenorhabditis elegans

Predicted to enable unfolded protein binding activity. Predicted to be involved in vacuolar proton-transporting V-type ATPase complex assembly. Located in endoplasmic reticulum.

let-350

Caenorhabditis elegans

Y102E9.6

Caenorhabditis elegans

Enriched in intestine; neurons; and in male based on RNA-seq and single-cell RNA-seq studies. Is affected by several genes including etr-1; csr-1; and drh-3 based on tiling array; microarray; and RNA-seq studies. Is predicted to encode a protein with the following domains: Secreted clade V proteins and Secreted clade V protein.

vha-15

Caenorhabditis elegans

Predicted to enable proton-transporting ATPase activity, rotational mechanism. Predicted to be involved in proton transmembrane transport. Predicted to be part of vacuolar proton-transporting V-type ATPase, V1 domain. Is an ortholog of human ATP6V1H (ATPase H+ transporting V1 subunit H).

C29E4.12

Caenorhabditis elegans

Predicted to be located in mitochondrion. Is an ortholog of human FMC1 (formation of mitochondrial complex V assembly factor 1 homolog) and FMC1-LUC7L2 (FMC1-LUC7L2 readthrough).

let-345

Caenorhabditis elegans

let-332

Caenorhabditis elegans

scvp-1

Caenorhabditis elegans

Enriched in male-specific anatomical entity based on microarray studies. Is affected by several genes including hsp-6; csr-1; and crh-1 based on RNA-seq and microarray studies. Is affected by nine chemicals including methylmercuric chloride; Tunicamycin; and Psoralens based on microarray and RNA-seq studies. Is predicted to encode a protein with the following domains: Secreted clade V proteins and Secreted clade V protein.